Atorvastatin Calcium Tablets USP, 80 mg, Rx Only, a). 90-count(NDC 67877-514-90), b).… Recall
Issued October 22, 2025 · Ascend Laboratories, LLC
In October 2025, Ascend Laboratories, LLC recalled the Atorvastatin Calcium Tablets USP, 80 mg, Rx Only, a). 90-count(NDC 67877-514-90), b).…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Dana Whitfield, RecallCheckr
What this means for you
Failed Dissolution Specifications
What you should do
- 1 Stop using Atorvastatin Calcium Tablets USP, 80 mg, Rx Only, a). 90-count(NDC 67877-514-90), b).… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Ascend Laboratories, LLC to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Recall details
- Brand
- Ascend Laboratories, LLC
- Category
- Health
- Recall date
- October 22, 2025
- Units affected
- Not reported
- Sold at
- U.S. Nationwide
- Recall number
- FDA-D-0020-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Ascend Laboratories, LLC has 15 recalls in our database.
- We're tracking 3,707 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.